ptpn9[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3922903	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 73,511,558-73,706,292 , GRCh37 chr15: 75,724,505-75,919,237 , GRCh38 chr15: 75,432,164-75,626,896	PTPN9, LOC107984720, 3 more genes
nsv3895840	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 75,768,387-75,901,066 , GRCh38.p12 chr15: 75,476,046-75,608,725	PTPN9, LOC105370902, 2 more genes
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	PTPN9, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	PTPN9, RNU6-18P, 1442 more genes
nsv3913942	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 70,025,300-78,705,993 , NCBI36 chr15: 68,104,693-76,785,390 , GRCh37 chr15: 70,317,639-78,998,335	PTPN9, SNX33, 209 more genes
nsv6637477	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 74,353,736-77,884,397 , GRCh38.p12 chr15: 74,061,395-77,592,055	PTPN9, NRG4, 96 more genes
nsv7137210	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,943,184-76,085,232 , GRCh38.p12 chr15: 72,650,843-75,792,891	PTPN9, LOC105370892, 99 more genes
nsv3895410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,943,184-76,072,324 , GRCh38.p12 chr15: 72,650,843-75,779,983	PTPN9, UBL7-DT, 97 more genes
nsv3920020	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 72,685,231-75,727,625 , NCBI36 chr15: 70,764,625-73,807,021 , GRCh37 chr15: 72,977,572-76,019,966	PTPN9, STRA6, 91 more genes
nsv3914896	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,963,970-75,954,617 , GRCh38 chr15: 72,671,629-75,662,276 , NCBI36 chr15: 70,751,023-73,741,672	PTPN9, CYP1A1, 88 more genes
nsv6315505	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 74,398,068-76,054,094 , GRCh38.p12 chr15: 74,105,727-75,761,753	PTPN9, RPL36AP45, 62 more genes
nsv4729106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 74,398,162-76,054,094 , GRCh38.p12 chr15: 74,105,821-75,761,753	PTPN9, FAM219B, 62 more genes
nsv3911951	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 72,186,358-73,827,604 , GRCh37.p13 chr15: 74,399,305-76,040,549 , GRCh38.p12 chr15: 74,106,964-75,748,208	PTPN9, NEIL1, 60 more genes
nsv3895297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 75,078,195-75,862,756 , GRCh38.p12 chr15: 74,785,854-75,570,415	PTPN9, FAM219B, 33 more genes
nsv5380975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 75,596,353-76,103,430 , GRCh38.p12 chr15: 75,304,012-75,811,089	PTPN9, RPL13P4, 20 more genes
nsv3916409	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 73,322,401-73,827,604 , GRCh37.p13 chr15: 75,535,348-76,040,549 , GRCh38.p12 chr15: 75,243,007-75,748,208	PTPN9, DNM1P34, 21 more genes
nsv4349273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 75,648,132-76,102,251 , GRCh38.p12 chr15: 75,355,791-75,809,910	PTPN9, SNUPN, 17 more genes
nsv491514	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr15: 72,671,374-75,680,568 , GRCh37 chr15: 72,963,715-75,972,909	PTPN9, BBS4, 91 more genes
nsv3900281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337	PTPN9, MYZAP, 1750 more genes
nsv3913581	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189	PTPN9, MIR4513, 1754 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 51

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Number of Variants: 20

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Search details

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